FUNGINIX ANTI-FUNGAL TREATMENT

Product NDC
71229-102
11-digit product format
712290102
Labeler code
71229
Product ID
71229-102_334f9228-a724-db45-e063-6394a90ad26b
Type
HUMAN OTC DRUG
Nonproprietary name
UNDECYLENIC ACID
Dosage form
OINTMENT
Route
TOPICAL
Labeler
The Sisquoc Healthcare Corporation
Application
M005
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-03-25
Substance
UNDECYLENIC ACID
Active strength
10 g/100mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
FUNGINIX ANTI-FUNGAL TREATMENT
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
UNDECYLENIC ACID10 g/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiK3D86KJ24N

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71229-102-11FUNGINIX ANTI-FUNGAL TREATMENT30 mL in 1 TUBEOINTMENT308

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71229-102FUNGINIX ANTI-FUNGAL TREATMENT (UNDECYLENIC ACID) OINTMENT [THE SISQUOC HEALTHCARE CORPORATION]8Current NDC, Legacy NDC, 1 package rows20250423_92db5433-5a1b-4cb9-b8eb-217c2a807a99.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71229-102-117122901021130 mL in 1 TUBE (71229-102-11) 30 ml2019-03-250000-00-00NoNoCurrent